Ekaterina L Ivanova
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Explore the profile of Ekaterina L Ivanova including associated specialties, affiliations and a list of published articles.
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9
Citations
110
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Recent Articles
1.
Ho K, Trapp M, Guida C, Ivanova E, De Jaime-Soguero A, Jabali A, et al.
Neuro Oncol
. 2024 Aug;
27(1):106-122.
PMID: 39215664
Background: The choroid plexus (ChP) is the secretory epithelial structure located in the brain ventricles. Choroid plexus tumors (CPTs) are rare neoplasms predominantly occurring in young patients with intensified malignancy...
2.
Ivanova E, Costa B, Eisemann T, Lohr S, Boskovic P, Eichwald V, et al.
Front Oncol
. 2022 Aug;
12:969787.
PMID: 35992852
Glioblastoma multiforme (GBM) is one of the most common and malignant brain tumors in adulthood with a median survival of only 15 months. This poor prognosis is related to GBM's...
3.
Costa B, Fletcher M, Boskovic P, Ivanova E, Eisemann T, Lohr S, et al.
Cancers (Basel)
. 2021 Jan;
13(2).
PMID: 33435218
Glioblastomas (GBM) are the most aggressive tumors affecting the central nervous system in adults, causing death within, on average, 15 months after diagnosis. Immunocompetent in-vivo models that closely mirror human...
4.
Gilet J, Ivanova E, Trofimova D, Rudolf G, Meziane H, Broix L, et al.
Hum Mol Genet
. 2020 Jan;
29(5):766-784.
PMID: 31919497
By using the Cre-mediated genetic switch technology, we were able to successfully generate a conditional knock-in mouse, bearing the KIF2A p.His321Asp missense point variant, identified in a subject with malformations...
5.
Carapito R, Ivanova E, Morlon A, Meng L, Molitor A, Erdmann E, et al.
Am J Hum Genet
. 2019 Dec;
106(1):137.
PMID: 31879022
No abstract available.
6.
Ivanova E, Gilet J, Sulimenko V, Duchon A, Rudolf G, Runge K, et al.
Nat Commun
. 2019 May;
10(1):2129.
PMID: 31086189
De novo heterozygous missense variants in the γ-tubulin gene TUBG1 have been linked to human malformations of cortical development associated with intellectual disability and epilepsy. Here, we investigated through in-utero...
7.
Carapito R, Ivanova E, Morlon A, Meng L, Molitor A, Erdmann E, et al.
Am J Hum Genet
. 2019 Jan;
104(2):319-330.
PMID: 30639322
ZMIZ1 is a coactivator of several transcription factors, including p53, the androgen receptor, and NOTCH1. Here, we report 19 subjects with intellectual disability and developmental delay carrying variants in ZMIZ1....
8.
Broix L, Asselin L, Silva C, Ivanova E, Tilly P, Gilet J, et al.
Hum Mol Genet
. 2017 Oct;
27(2):224-238.
PMID: 29077851
Genetic findings reported by our group and others showed that de novo missense variants in the KIF2A gene underlie malformations of brain development called pachygyria and microcephaly. Though KIF2A is...
9.
Ivanova E, Mau-Them F, Riazuddin S, Kahrizi K, Laugel V, Schaefer E, et al.
Am J Hum Genet
. 2017 Aug;
101(3):428-440.
PMID: 28823707
Pontocerebellar hypoplasia (PCH) is a heterogeneous group of rare recessive disorders with prenatal onset, characterized by hypoplasia of pons and cerebellum. Mutations in a small number of genes have been...